N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine

Base Information

• Chemical Name: N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine
• CAS No.: 1269527-19-6
• Molecular Formula: C₁₈H₁₆ClN₇S
• Molecular Weight: 397.891

Synonyms:N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine

Chemical Property of N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine

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Technology Process of N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine

There total 4 articles about N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 49.0%

6-(chloromethyl)-N2-(4-chlorophenyl)-1,3,5-triazine-2,4-diamine (30355-61-4) + 5-methyl-2-benz-1,3-imidazoline-2-thione (27231-36-3) → N2-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine (1269527-19-6)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

DOI:10.1007/s00044-011-9574-8

Reference yield:

1-(4-chlorophenyl)biguanide hydrochloride (4022-81-5,55307-40-9) → N2-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine (1269527-19-6)

Guidance literature:

Multi-step reaction with 2 steps

1.1: sodium methylate / methanol / 3 h / 20 °C

1.2: 48 h / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

With sodium methylate; potassium carbonate; In methanol; N,N-dimethyl-formamide;

DOI:10.1007/s00044-011-9574-8

Reference yield:

4-chloro-aniline (106-47-8) → N2-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine (1269527-19-6)

Guidance literature:

Multi-step reaction with 3 steps

1.1: hydrogenchloride / water / Reflux

2.1: sodium methylate / methanol / 3 h / 20 °C

2.2: 48 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogenchloride; sodium methylate; potassium carbonate; In methanol; water; N,N-dimethyl-formamide;

DOI:10.1007/s00044-011-9574-8

upstream raw materials:

6-(chloromethyl)-N²-(4-chlorophenyl)-1,3,5-triazine-2,4-diamine

5-methyl-2-benz-1,3-imidazoline-2-thione

1-(4-chlorophenyl)biguanide hydrochloride

4-chloro-aniline

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